A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020015



Internal ID19109234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18777092..19107771hg38UCSC Ensembl
Innerchr5:18777201..19107880hg19UCSC Ensembl
Innerchr5:18812958..19143637hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38330680
hg19330680
hg18330680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5594n100
Supporting Variantsnssv3745827, nssv3635894, nssv3635893
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020015
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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